苏州药明康德新药开发股份有限公司
企业性质： 员工人数：人 所属行业：
企业性质： 员工人数：人 所属行业：
职位类别：
Conduct inspections/audits of studies, facilities, processes, systems and vendors, report observations to management, and maintain complete inspection/audit files on assigned studies/projects; 2. Schedule/conduct inspections of QA activities; 3. Audit study protocols and final reports and associated amendments and prepare QAU statements for final reports within all GLP areas; 4. Review line function SOPs for compliance with GLP regulations； 5. Maintain QA records and Master Schedule and implement and support QA trend analysis. 任职资格：1. Degree in Natural Sciences or comparable related experience； 2. Good interpersonal and communication (written and oral) skills； 3. Good understanding both written and oral of English language； 4. Understanding of regulatory (GLP) requirements. 5. Have computerized system validation experience is better;
苏州药明康德通过赋能全球制药、生物科技和医疗器械公司，药明康德致力于推动新药研发进程，为患者带来突破性的治疗方案。本着以研究为首任，以客户为中心的宗旨，药明康德通过高性价比和高效的研发服务，助力客户提升研发效率，服务范围涵盖化学药研发和生产、细胞及基因疗法研发生产、医疗器械测试等领域。目前，药明康德的赋能平台正承载着来自全球 30 多个国家的 4000 多家合作伙伴的研发创新项目，致力于将更多新药、好药带给全球病患，早日实现“让天下没有难做的药，难治的病”的愿景。